A 2-week Clinical Comparison of SYSTANE® Ultra to Sensitive Eyes Rewetting Drops in Contact Lens Wearing Patients.
NCT ID: NCT00769665
Last Updated: 2012-02-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
47 participants
OBSERVATIONAL
2008-10-31
2009-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Systane Ultra
Systane Ultra
Systane Ultra
Re-wetting ocular eye drop
Sensitive Eyes
Sensitive Eyes
Sensitive Eyes Rewetting Drops
Re-wetting ocular eye drop
Interventions
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Systane Ultra
Re-wetting ocular eye drop
Sensitive Eyes Rewetting Drops
Re-wetting ocular eye drop
Eligibility Criteria
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Inclusion Criteria
* Provide written Informed Consent.
* Must be wearing a planned replacement soft lens in a 2 week or monthly replacement modality, or a Rigid Gas Permeable (RGP) contact Lens
* Must have best corrected distance visual acuity, with contact lenses, of 20/30 or better in each eye.
* Sodium fluorescein (NaFl) corneal staining score sum of \< 2 in both eyes (NEI scoring system).
* Must be willing to maintain pre-enrollment systemic medication regimens during the study.
* Must be available for study visits and to fill out study questionnaires.
Exclusion Criteria
* Has a history of allergy to any study product ingredients
* Is unwilling or unable to meet the study visit timeline.
* Has any active corneal, eyelid or other anterior segment inflammation or infection, which, in the opinion of the Investigator, would adversely affect successful contact lens wear.
* Is currently using any topical eye medications (not including rewetting drops, artificial tear products or Restasis).
18 Years
ALL
Yes
Sponsors
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Alcon Research
INDUSTRY
Responsible Party
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Other Identifiers
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SMA-08-15
Identifier Type: -
Identifier Source: org_study_id
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